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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:43997 -
N
6
,
N
6
-
dimethyl-
L
-
lysine
Main
ChEBI Ontology
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ChEBI Name
N
6
,
N
6
-
dimethyl-
L
-
lysine
ChEBI ID
CHEBI:43997
ChEBI ASCII Name
N(6),N(6)-dimethyl-L-lysine
Definition
An
L
-lysine derivative comprising
L
-lysine having two methyl substituents attached to the side-chain amino group.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:43992, CHEBI:21855
Supplier Information
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Formula
C8H18N2O2
Net Charge
0
Average Mass
174.24070
Monoisotopic Mass
174.13683
InChI
InChI=1S/C8H18N2O2/c1-10(2)6-4-3-5-7(9)8(11)12/h7H,3-6,9H2,1-2H3,(H,11,12)/t7-/m0/s1
InChIKey
XXEWFEBMSGLYBY-ZETCQYMHSA-N
SMILES
CN(C)CCCC[C@H](N)C(O)=O
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
6
,
N
6
-
dimethyl-
L
-
lysine (
CHEBI:43997
)
is a
L
-lysine derivative (
CHEBI:25095
)
N
6
,
N
6
-
dimethyl-
L
-
lysine (
CHEBI:43997
)
is a
non-proteinogenic
L
-α-amino acid (
CHEBI:83822
)
N
6
,
N
6
-
dimethyl-
L
-
lysine (
CHEBI:43997
)
is conjugate base of
N
6
,N
6
-dimethyl-
L
-lysinium (
CHEBI:193107
)
Incoming
N
6
,N
6
-dimethyl-
L
-lysinium (
CHEBI:193107
)
is conjugate acid of
N
6
,
N
6
-
dimethyl-
L
-
lysine (
CHEBI:43997
)
N
6
,
N
6
-dimethyl-
L
-lysine residue (
CHEBI:61969
)
is substituent group from
N
6
,
N
6
-
dimethyl-
L
-
lysine (
CHEBI:43997
)
IUPAC Name
N
6
,
N
6
-
dimethyl-
L
-
lysine
Synonyms
Sources
(
S
)-2-amino-6-dimethylaminohexanoic acid
ChEBI
Epsilon N-dimethyllysine
ChemIDplus
Lys(Me
2
)
ChEBI
N(6),N(6)-Dimethyl-L-lysine
ChemIDplus
N
6
,
N
6
-dimethyllysine
ChEBI
N
ε
,
N
ε
-
dimethyl-
L
-
lysine
ChEBI
N
ε
,
N
ε
-dimethyllysine
ChEBI
N
ε
-dimethyl-
L
-lysine
ChEBI
N
ε
-dimethyllysine
ChEBI
Manual Xref
Database
MLY
PDBeChem
View more database links
Registry Numbers
Types
Sources
2259-86-1
CAS Registry Number
ChemIDplus
2355193
Reaxys Registry Number
Reaxys
Citations
Types
Sources
2504290
PubMed citation
Europe PMC
3773934
PubMed citation
Europe PMC
5212577
PubMed citation
Europe PMC
6450198
PubMed citation
Europe PMC
6863304
PubMed citation
Europe PMC
Last Modified
16 December 2014